Experimental infection with Cryptosporidium parvum IIaA21G1R1 subtype in immunosuppressed mice

被引:11
作者
Del Coco, Valeria F. [1 ,2 ]
Cordoba, Maria A. [1 ,3 ]
Sidoti, Alicia [4 ]
Santin, Monica [5 ]
Drut, Ricardo [4 ]
Basualdo, Juan A. [1 ]
机构
[1] Univ Nacl La Plata, Fac Ciencias Med, Catedra Microbiol & Parasitol, RA-1900 La Plata, Buenos Aires, Argentina
[2] Consejo Nacl Invest Cient & Tecn CONICET, La Plata, Buenos Aires, Argentina
[3] Comis Invest Cient Prov Buenos Aires, RA-1900 La Plata, Buenos Aires, Argentina
[4] Univ Nacl La Plata, Fac Ciencias Med, Catedra Patol A, RA-1900 La Plata, Buenos Aires, Argentina
[5] USDA ARS, Environm Microbial & Food Safety Lab, Anim & Nat Resources Inst, Beltsville, MD 20705 USA
关键词
Cryptosporidium parvum; Apoptosis; Immunosuppression; Murine model; CELL RENEWAL; DAIRY-CATTLE; MOUSE MODEL; WEIGHT-LOSS; APOPTOSIS; OOCYSTS; DEFICIENT; RESPONSES; AGE;
D O I
10.1016/j.vetpar.2012.06.033
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Cryptosporidium parvum subtype IIaA21G1R1 oocysts were used to infect dexamethasone immunosuppressed N: NIH Swiss mice. This is the first Cryptosporidium mouse model in which the relationship between infection and apoptosis has been histologically studied at each portion of the gut in order to observe this dynamic in chronic cryptosporidiosis. Histology showed developmental stages in the duodenum, proximal and distal jejunum, ileum, cecum and colon, with the small intestine remaining infected until day 35 post infection. At proximal jejunum an inverse correlation between infection and apoptosis was observed at days 28 and 35 p.i. Data suggests that jejunum could be an interesting place to carry out further studies on the dynamics of Cryptosporidium infection and apoptosis. Based on these findings, this mouse model was useful to evaluate clinical, parasitological and histological aspects of C. parvum subtype IIaA21G1R1 infection, and it will be an appropriate tool to investigate different aspects of Cryptosporidium infection. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:411 / 417
页数:7
相关论文
共 35 条
[1]  
[Anonymous], 1996, GUID CAR US LAB AN
[2]   EFFECT OF 3 CONCENTRATION TECHNIQUES ON VIABILITY OF CRYPTOSPORIDIUM-PARVUM OOCYSTS RECOVERED FROM BOVINE FECES [J].
BUKHARI, Z ;
SMITH, HV .
JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (10) :2592-2595
[3]  
Certad G., 2007, INFECT AGENTS CANC, V21, P2
[4]   Zoonotic cryptosporidiosis in the UK - challenges for control [J].
Chalmers, R. M. ;
Giles, M. .
JOURNAL OF APPLIED MICROBIOLOGY, 2010, 109 (05) :1487-1497
[5]   Cryptosporidium parvum induces apoptosis in biliary epithelia by a Fas/Fas ligand-dependent mechanism [J].
Chen, XM ;
Gores, GJ ;
Paya, CV ;
LaRusso, NF .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1999, 277 (03) :G599-G608
[6]   Host intestinal epithelial response to Cryptosporidium parvum [J].
Deng, MQ ;
Rutherford, MS ;
Abrahamsen, MS .
ADVANCED DRUG DELIVERY REVIEWS, 2004, 56 (06) :869-884
[7]  
EDWARDS JL, 1961, AM J PATHOL, V38, P437
[8]   Pathogenicity of Cryptosporidium parvum -: evaluation of an animal infection model [J].
Enemark, HL ;
Bille-Hansen, V ;
Lind, P ;
Heegaard, PMH ;
Vigre, H ;
Ahrens, P ;
Thamsborg, SM .
VETERINARY PARASITOLOGY, 2003, 113 (01) :35-57
[9]  
Fayer Ronald, 2008, P1
[10]   Infection of immunocompetent mice with acid-water-pretreated Cryptosporidium parvum results in weight loss, and intestinal (structural and physiological) alterations [J].
Garza, Armandina ;
Castenallos-Gonzalez, Alejandro ;
Griffiths, Jeffrey ;
Robinson, Prema .
PARASITOLOGY RESEARCH, 2008, 102 (03) :457-463